Acheiropodia
| Acheiropodia | |
|---|---|
| Synonyms | N/A |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Congenital absence of hands and feet |
| Complications | N/A |
| Onset | Birth |
| Duration | Lifelong |
| Types | N/A |
| Causes | Genetic mutation |
| Risks | N/A |
| Diagnosis | Clinical examination, Genetic testing |
| Differential diagnosis | N/A |
| Prevention | N/A |
| Treatment | Supportive care |
| Medication | N/A |
| Prognosis | N/A |
| Frequency | Rare disease |
| Deaths | N/A |
Acheiropodia is a rare genetic disorder characterized by the congenital absence of hands and feet. This condition is inherited in an autosomal recessive pattern and is caused by mutations in the LMBR1 gene.
Presentation[edit]
Individuals with acheiropodia are born without hands and feet, a condition known as amelia. The absence of these limbs is due to a disruption in the normal development of the limb bud during embryogenesis.
Genetics[edit]
Acheiropodia is caused by mutations in the LMBR1 gene, which is located on chromosome 7. This gene is involved in the sonic hedgehog signaling pathway, which plays a crucial role in the development of limbs. The condition follows an autosomal recessive inheritance pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.
Diagnosis[edit]
Diagnosis of acheiropodia is primarily based on clinical examination and the characteristic absence of hands and feet. Genetic testing can confirm the diagnosis by identifying mutations in the LMBR1 gene.
Management[edit]
There is no cure for acheiropodia, and management focuses on supportive care to improve the quality of life for affected individuals. This may include the use of prosthetic devices, physical therapy, and occupational therapy to enhance mobility and independence.
Epidemiology[edit]
Acheiropodia is an extremely rare condition, with only a few cases reported in the medical literature. It is more commonly observed in certain isolated populations where consanguinity is more prevalent.
See also[edit]
References[edit]
<references />
External links[edit]
Acheiropodia[edit]
-
Autorecessive
-
Acheiropodia Mutation
-
Acheiropodia Chromatin Architecture (TAD)
Ad. Transform your life with W8MD's
GLP-1 weight loss injections special from $29.99 with insurance
|
WikiMD Medical Encyclopedia |
Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian